Down-modulation of nucleoporin RanBP2/Nup358 impaired chromosomal alignment and induced mitotic catastrophe

Cell Death Dis. 2013 Oct 10;4(10):e854. doi: 10.1038/cddis.2013.370.

Abstract

Chromosomal missegregation is a common feature of many human tumors. Recent studies have indicated a link between nucleoporin RanBP2/Nup358 and chromosomal segregation during mitosis; however, the molecular details have yet to be fully established. Observed through live cell imaging and flow cytometry, here we show that RNA interference-mediated knockdown of RanBP2 induced G2/M phase arrest, metaphase catastrophe and mitotic cell death. Furthermore, RanBP2 down-modulation disrupted importin/karyopherin β1 as well as the expression and localization of the Ran GTPase activating protein 1. We found that N-terminal of RanBP2 interacted with the N-terminal of importin β1. Moreover, at least a portion of RanBP2 partially localizes at the centrosome during mitosis. Notably, we also found that GTPase Ran is also involved in the regulation of RanBP2-importin β1 interaction. Overall, our results suggest that mitotic arrest and the following cell death were caused by depletion of RanBP2. Our findings point to a crucial role for RanBP2 in proper mitotic progression and faithful chromosomal segregation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Aneuploidy
  • Cell Death
  • Cell Nucleus / metabolism
  • Centrosome / metabolism
  • Chromosomes, Human / metabolism*
  • Down-Regulation*
  • G2 Phase
  • Gene Knockdown Techniques
  • HeLa Cells
  • Humans
  • Karyopherins / chemistry
  • Karyopherins / metabolism
  • Kinetochores / metabolism
  • Mitosis*
  • Models, Biological
  • Molecular Chaperones / chemistry
  • Molecular Chaperones / metabolism*
  • Nuclear Pore Complex Proteins / chemistry
  • Nuclear Pore Complex Proteins / metabolism*
  • Protein Binding
  • Protein Transport
  • RNA, Small Interfering / metabolism

Substances

  • Karyopherins
  • Molecular Chaperones
  • Nuclear Pore Complex Proteins
  • RNA, Small Interfering
  • ran-binding protein 2